Cargando…

“Activated Borane”: A Porous Borane Cluster Polymer as an Efficient Lewis Acid-Based Catalyst

[Image: see text] Borane cluster-based porous covalent networks, named activated borane (ActB), were prepared by cothermolysis of decaborane(14) (nido-B(10)H(14)) and selected hydrocarbons (toluene, ActB-Tol; cyclohexane, ActB-cyHx; and n-hexane, ActB-nHx) under anaerobic conditions. These amorphous...

Descripción completa

Detalles Bibliográficos
Autores principales: Lamač, Martin, Urbán, Béla, Horáček, Michal, Bůžek, Daniel, Leonová, Lucie, Stýskalík, Aleš, Vykydalová, Anna, Škoch, Karel, Kloda, Matouš, Mahun, Andrii, Kobera, Libor, Lang, Kamil, Londesborough, Michael G. S., Demel, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660343/
https://www.ncbi.nlm.nih.gov/pubmed/38026813
http://dx.doi.org/10.1021/acscatal.3c04011
Descripción
Sumario:[Image: see text] Borane cluster-based porous covalent networks, named activated borane (ActB), were prepared by cothermolysis of decaborane(14) (nido-B(10)H(14)) and selected hydrocarbons (toluene, ActB-Tol; cyclohexane, ActB-cyHx; and n-hexane, ActB-nHx) under anaerobic conditions. These amorphous solid powders exhibit different textural and Lewis acid (LA) properties that vary depending on the nature of the constituent organic linker. For ActB-Tol, its LA strength even approaches that of the commonly used molecular LA, B(C(6)F(5))(3). Most notably, ActBs can act as heterogeneous LA catalysts in hydrosilylation/deoxygenation reactions with various carbonyl substrates as well as in the gas-phase dehydration of ethanol. These studies reveal the potential of ActBs in catalytic applications, showing (a) the possibility for tuning catalytic reaction outcomes (selectivity) in hydrosilylation/deoxygenation reactions by changing the material’s composition and (b) the very high activity toward ethanol dehydration that exceeds the commonly used γ-Al(2)O(3) by achieving a stable conversion of ∼93% with a selectivity for ethylene production of ∼78% during a 17 h continuous period on stream at 240 °C.